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Date	Panel	Item	Activity
Filter activities 9 actions
20 Jan 2022	Fetal anomalies v0.2533	TRPV3	Zornitza Stark Marked gene: TRPV3 as ready
20 Jan 2022	Fetal anomalies v0.2533	TRPV3	Zornitza Stark Gene: trpv3 has been classified as Red List (Low Evidence).
20 Jan 2022	Fetal anomalies v0.2533	TRPV3	Zornitza Stark Phenotypes for gene: TRPV3 were changed from OLMSTED SYNDROME to Olmsted syndrome 1, MIM# 614594
13 Jan 2022	Fetal anomalies v0.2009	TRPV3	Chirag Patel Classified gene: TRPV3 as Red List (low evidence)
13 Jan 2022	Fetal anomalies v0.2009	TRPV3	Chirag Patel Gene: trpv3 has been classified as Red List (Low Evidence).
13 Jan 2022	Fetal anomalies v0.2009	TRPV3	Chirag Patel Classified gene: TRPV3 as Red List (low evidence)
13 Jan 2022	Fetal anomalies v0.2009	TRPV3	Chirag Patel Gene: trpv3 has been classified as Red List (Low Evidence).
13 Jan 2022	Fetal anomalies v0.2008	TRPV3	Chirag Patel reviewed gene: TRPV3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
24 Oct 2021	Fetal anomalies v0.0	TRPV3	Zornitza Stark gene: TRPV3 was added gene: TRPV3 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: TRPV3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: TRPV3 were set to OLMSTED SYNDROME